Canonical Allele Identifier: CA445803879

Gene: SLC25A46

Linked Data

• dbSNP Id: rs1800242296
• MyVariant Identifiers: chr5:g.110096981G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761281G>A , CM000667.2:g.110761281G>A	GRCh38
NC_000005.9:g.110096981G>A , CM000667.1:g.110096981G>A	GRCh37
NC_000005.8:g.110124880G>A	NCBI36
NG_051334.1:g.28146G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.756G>A MANE Select	ENSP00000348211.3:p.Val252=
ENST00000355943.7:c.756G>A	ENSP00000348211.3:p.Val252=
ENST00000447245.6:c.679-166G>A	ENSP00000399717.2:n.679-166G>A
ENST00000502462.6:n.1072G>A
ENST00000504098.1:c.318G>A	ENSP00000425708.1:p.Val106=
ENST00000509432.1:c.117G>A	ENSP00000426604.1:p.Val39=
ENST00000513706.2:n.2356G>A
ENST00000513807.5:c.270G>A	ENSP00000421134.1:p.Val90=
NM_001303249.1:c.679-166G>A	NP_001290178.1:n.679-166G>A
NM_001303250.1:c.483G>A	NP_001290179.1:p.Val161=
NM_138773.2:c.756G>A	NP_620128.1:p.Val252=
NM_001303249.2:c.679-166G>A	NP_001290178.1:n.679-166G>A
NM_001303250.2:c.483G>A	NP_001290179.1:p.Val161=
NM_138773.3:c.756G>A	NP_620128.1:p.Val252=
NR_138151.1:n.1030G>A
NM_138773.4:c.756G>A MANE Select	NP_620128.1:p.Val252=
NM_001303249.3:c.679-166G>A	NP_001290178.1:n.679-166G>A
NM_001303250.3:c.483G>A	NP_001290179.1:p.Val161=
NR_138151.2:n.995G>A